785 reports of this reaction
3.2% of all TOLVAPTAN reports
#4 most reported adverse reaction
CARDIAC FAILURE is the #4 most commonly reported adverse reaction for TOLVAPTAN, manufactured by Otsuka America Pharmaceutical, Inc.. There are 785 FDA adverse event reports linking TOLVAPTAN to CARDIAC FAILURE. This represents approximately 3.2% of all 24,584 adverse event reports for this drug.
Patients taking TOLVAPTAN who experience cardiac failure should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
CARDIAC FAILURE is moderately reported among TOLVAPTAN users, representing a notable but not dominant share of adverse events.
In addition to cardiac failure, the following adverse reactions have been reported for TOLVAPTAN:
The following drugs have also been linked to cardiac failure in FDA adverse event reports:
CARDIAC FAILURE has been reported as an adverse event in 785 FDA reports for TOLVAPTAN. This does not prove causation, but indicates an association observed in post-market surveillance data.
CARDIAC FAILURE accounts for approximately 3.2% of all adverse event reports for TOLVAPTAN, making it a notable side effect.
If you experience cardiac failure while taking TOLVAPTAN, contact your healthcare provider. They can evaluate whether the symptom is related to your medication and discuss potential adjustments to your treatment plan. Do not stop taking prescribed medication without consulting your doctor.